Restoring Visual Function to Blind Mice with a Photoswitch that Exploits Electrophysiological Remodeling of Retinal Ganglion Cells

Retinitis pigmentosa (RP) and age-related macular degeneration (AMD) are blinding diseases caused by the degeneration of rods and cones, leaving the remainder of the visual system unable to respond to light. Here, we report a chemical photoswitch named DENAQ that restores retinal responses to white light of intensity similar to ordinary daylight. A single intraocular injection of DENAQ photosensitizes the blind retina for days, restoring electrophysiological and behavioral responses with no toxicity. Experiments on mouse strains with functional, nonfunctional, or degenerated rods and cones show that DENAQ is effective only in retinas with degenerated photoreceptors. DENAQ confers light sensitivity on a hyperpolarization-activated inward current that is enhanced in degenerated retina, enabling optical control of retinal ganglion cell firing. The acceptable light sensitivity, favorable spectral sensitivity, and selective targeting to diseased tissue make DENAQ a prime drug candidate for vision restoration in patients with end-stage RP and AMD.

[1]  S Berman,et al.  Retinal damage by light in rats. , 1966, Investigative ophthalmology.

[2]  Xing Wu,et al.  Is ZD7288 a selective blocker of hyperpolarization-activated cyclic nucleotide-gated channel currents? , 2012, Channels.

[3]  A. Ishida,et al.  Colocalization of hyperpolarization‐activated, cyclic nucleotide‐gated channel subunits in rat retinal ganglion cells , 2011, The Journal of comparative neurology.

[4]  Martin Biel,et al.  Exploring HCN channels as novel drug targets , 2011, Nature Reviews Drug Discovery.

[5]  Jessy D. Dorn,et al.  Interim results from the international trial of Second Sight's visual prosthesis. , 2012, Ophthalmology.

[6]  E J Chichilnisky,et al.  Changes in physiological properties of rat ganglion cells during retinal degeneration. , 2011, Journal of neurophysiology.

[7]  Kwoon Y. Wong,et al.  Synaptic influences on rat ganglion‐cell photoreceptors , 2007, The Journal of physiology.

[8]  Eberhart Zrenner,et al.  Photoreceptor Cell Death Mechanisms in Inherited Retinal Degeneration , 2008, Molecular Neurobiology.

[9]  B. Jones,et al.  Retinal remodeling , 2012, Japanese Journal of Ophthalmology.

[10]  Dirk Trauner,et al.  Tuning photochromic ion channel blockers. , 2011, ACS chemical neuroscience.

[11]  S. Nonell,et al.  Fastest thermal isomerization of an azobenzene for nanosecond photoswitching applications under physiological conditions. , 2012, Angewandte Chemie.

[12]  Karl Deisseroth,et al.  Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa , 2010, Science.

[13]  A. Ramé [Age-related macular degeneration]. , 2006, Revue de l'infirmiere.

[14]  Tiansen Li,et al.  Retinal degeneration in the rd mouse is caused by a defect in the β subunit of rod cGMP-phosphodiesterase , 1990, Nature.

[15]  A. Milam,et al.  Histopathology of the human retina in retinitis pigmentosa. , 1998, Progress in retinal and eye research.

[16]  T. Reh,et al.  Transplantation of human embryonic stem cell-derived photoreceptors restores some visual function in Crx-deficient mice. , 2009, Cell stem cell.

[17]  Timothy W. Dunn,et al.  Photochemical control of endogenous ion channels and cellular excitability , 2008, Nature Methods.

[18]  M. Fiore,et al.  Postnatal changes in nerve growth factor and brain derived neurotrophic factor levels in the retina, visual cortex, and geniculate nucleus in rats with retinitis pigmentosa , 2003, Neuroscience Letters.

[19]  S. Stasheff,et al.  Emergence of sustained spontaneous hyperactivity and temporary preservation of OFF responses in ganglion cells of the retinal degeneration (rd1) mouse. , 2008, Journal of neurophysiology.

[20]  David H. Sliney,et al.  The susceptibility of the retina to photochemical damage from visible light , 2012, Progress in Retinal and Eye Research.

[21]  D. Chetkovich,et al.  HCN channels in behavior and neurological disease: Too hyper or not active enough? , 2011, Molecular and Cellular Neuroscience.

[22]  Shigang He,et al.  Changing dendritic field size of mouse retinal ganglion cells in early postnatal development , 2010, Developmental neurobiology.

[23]  Douglas S Kim,et al.  Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration , 2008, Nature Neuroscience.

[24]  A. Rouvas,et al.  SAFETY OF REPEAT INTRAVITREAL INJECTIONS OF BEVACIZUMAB VERSUS RANIBIZUMAB: Our Experience After 2,000 Injections , 2009, Retina.

[25]  N. Rao,et al.  Disruption of the gene encoding the beta1-subunit of transducin in the Rd4/+ mouse. , 2006, Investigative ophthalmology & visual science.

[26]  S. Petersen-Jones Advances in the molecular understanding of canine retinal diseases. , 2005, The Journal of small animal practice.

[27]  S. Haverkamp,et al.  HCN channels are expressed differentially in retinal bipolar cells and concentrated at synaptic terminals , 2003, The European journal of neuroscience.

[28]  Dirk Trauner,et al.  LiGluR restores visual responses in rodent models of inherited blindness. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

[29]  J. Haller,et al.  The dexamethasone drug delivery system: Indications and evidence , 2011, Advances in therapy.

[30]  Jian-Guo Chen,et al.  Aquaporin-4 Deficiency Impairs Synaptic Plasticity and Associative Fear Memory in the Lateral Amygdala: Involvement of Downregulation of Glutamate Transporter-1 Expression , 2012, Neuropsychopharmacology.

[31]  T H Roderick,et al.  A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse. , 1997, Genomics.

[32]  R. Kramer,et al.  Light at the end of the channel: optical manipulation of intrinsic neuronal excitability with chemical photoswitches , 2013, Front. Mol. Neurosci..

[33]  S. Schwartz,et al.  Embryonic stem cell trials for macular degeneration: a preliminary report , 2012, The Lancet.

[34]  Dirk Trauner,et al.  Photochemical Restoration of Visual Responses in Blind Mice , 2012, Neuron.

[35]  Konrad Lehmann,et al.  Visual Function in Mice with Photoreceptor Degeneration and Transgenic Expression of Channelrhodopsin 2 in Ganglion Cells , 2010, The Journal of Neuroscience.

[36]  Sherwin C. Lee,et al.  Ih without Kir in adult rat retinal ganglion cells. , 2007, Journal of neurophysiology.

[37]  Michael A. Henninger,et al.  High-Performance Genetically Targetable Optical Neural Silencing via Light-Driven Proton Pumps , 2010 .

[38]  A. Milam,et al.  Rhodopsin transgenic pigs as a model for human retinitis pigmentosa. , 1998, Investigative ophthalmology & visual science.

[39]  A. Felipe,et al.  Spectral transmission of the human crystalline lens in adult and elderly persons: color and total transmission of visible light. , 2012, Investigative ophthalmology & visual science.

[40]  M. Biel,et al.  Melanopsin and rod–cone photoreceptive systems account for all major accessory visual functions in mice , 2003, Nature.

[41]  Paula C. Stacey,et al.  Effectiveness of computer-based auditory training for adult users of cochlear implants , 2010, International journal of audiology.

[42]  S. Siegelbaum,et al.  TRIP8b Splice Variants Form a Family of Auxiliary Subunits that Regulate Gating and Trafficking of HCN Channels in the Brain , 2009, Neuron.

[43]  E. Fischer,et al.  Wavelength Dependence of Photoisomerization Equilibria in Azocompounds , 1955 .

[44]  D. Loo,et al.  In situ detection of apoptosis by the TUNEL assay: an overview of techniques. , 2011, Methods in molecular biology.

[45]  B. Jones,et al.  Neural remodeling in retinal degeneration , 2003, Progress in Retinal and Eye Research.

[46]  Alice K. Cho,et al.  Retinal prostheses: current clinical results and future needs. , 2011, Ophthalmology.

[47]  G. Ying,et al.  Ranibizumab and bevacizumab for treatment of neovascular age-related macular degeneration: two-year results. , 2012, Ophthalmology.